gudid
Primary ID: SBS105
Swiss Bi-Manual I/A (UDI SBS105)
Manufactured by Medicel AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Swiss Bi-Manual I/A - Primary ID SBS105
Device Regulatory Overview
The Swiss Bi-Manual I/A (Model/Catalog Number: SBS105) is a medical device manufactured by Medicel AG. This product is indexed under FDA Product Code / Category Classification HMX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SBS105
- Product Code / EMDN
- HMX
- Device Name
- The Irrigation-/Aspiration-Handpieces are used to remove the opaque human lens during cataract surgery.
- Database Sync Date
- 2026-08-09 09:03:20
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Swiss Bi-Manual I/A?
The registered manufacturer of record for Swiss Bi-Manual I/A is Medicel AG.
What is the Primary UDI-DI identifier for Swiss Bi-Manual I/A?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SBS105.
What classification code is assigned to this device?
This device is registered under product classification code HMX.
Similar Classification Devices (HMX)
Other Devices by Medicel AG
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